FDA UDI In Commercial Distribution 🇺🇸 United States

VA-LCP

DI: 10886982261663 · Model: 03.111.120S · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
VA-LCP
Primary DI
10886982261663
Version / Model
03.111.120S
Catalog Number
03111120S
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-14
Public Version
4
Public Version Date
2022-05-02
Public Version Status
Update
Public Device Record Key
efb62e8e-4fb5-44ed-811b-5097d820a041

Device Description

2.4MM VA LCP 2-COL DSTL RAD PL TEMPLATES - STERILE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWT TEMPLATE

GMDN Terms

Code Name
58804 Surgical implant template, single-use

Identifiers

Type ID
Primary 10886982261663

Customer Contacts